To compare the effectiveness of trans-cervical foley catheter and intravaginal Misoprostol in making the uterine cervix more favourable for induction of labour
Not Applicable
Suspended
- Conditions
- Effectiveness of trans-cervical foley catheter and intra-vaginal Misoprotol for pre induction cervical ripening
- Registration Number
- SLCTR/2008/002
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Suspended
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Consented women with singleton gestation in vertex presentation at greater than 28 weeks gestation with Bishop’s score less than 6
Exclusion Criteria
•Rupture of membranes antepartum bleeding •active genital herpes infection •fetal death •placenta praevia •previous induction or pre-induction agent during the pregnancy, and known allergy to misoprostol •Women with history of cesarean deliveries will not be excluded
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method